Micropillar-integrated device for monitoring dynamic regulation of traction forces during cell migration

Eijiro Maeda, A. Sugawara, J. Cooper-White, T. Ohashi
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Abstract

Cell migration plays an important role in many physiological and pathological processes such as morphogenesis, wound healing, and tumor metastasis. Although the majority of such events occur with cells moving as a group, called collective cell migration, mechanics of collective cell migrations has not been understood well compared to a single cell migration. Mechanical interactions between cells and their surroundings have been demonstrated to regulate cell migration. One of such interactions is the induction of traction forces by acto-myosin dynamics within cells to their local environment, as it has been reported that cells alter the magnitude of traction forces depending on the stiffness of attaching substrates. In connection with cell migration, it has also been demonstrated the importance of substrate stiffness during cell migration using microfabricated substrates consisting of arrays of micropillars. To understand the mechanics of collective cell migration, it is important to know how cells within a moving cell collectivity generate forces to move the collectivity forward at single cell level. Accordingly, the present study was performed to clarify the mechanics of collective cell migration by measuring traction forces exerted by mouse NIH 3T3 fibroblasts using a newly developed migration assay device.
用于监测细胞迁移过程中牵引力动态调节的微柱集成装置
细胞迁移在形态发生、创面愈合、肿瘤转移等生理病理过程中起着重要作用。尽管大多数此类事件发生在细胞作为一个群体移动时,称为集体细胞迁移,但与单个细胞迁移相比,集体细胞迁移的机制尚未得到很好的理解。细胞和周围环境之间的机械相互作用已被证明可以调节细胞迁移。其中一种相互作用是通过细胞内肌动蛋白动力学诱导牵引力到其局部环境,因为据报道,细胞根据附着底物的刚度改变牵引力的大小。在细胞迁移方面,使用由微柱阵列组成的微制造衬底也证明了衬底刚度在细胞迁移过程中的重要性。为了理解集体细胞迁移的机制,重要的是要知道一个移动的细胞集体中的细胞如何产生力量,使集体在单个细胞水平上向前移动。因此,本研究通过使用新开发的迁移实验装置测量小鼠NIH 3T3成纤维细胞施加的牵引力来阐明集体细胞迁移的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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